FDAFDA · Food and drugs·Recall number Z-0071-2019
smiths medical portex First Breath Adult Nasal Cannula, REF 001283, Non-flared Tips, 213 cm (7 ft.) Tubing, Over-the-Ear Style. Product Usage: For the administration of nasal oxygen and humidity to patients.
Published October 10, 2018 · Recall initiated: July 6, 2018
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
"Manufactured" and "Use By" labels are transposed incorrectly suggesting the product expires before it was manufactured.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Smiths Medical ASD Inc.
- Distributor
- Worldwide Distribution - US Nationwide in the states of AR, CA, GA, IN, LA, OK, MA, MI, NC, NJ, NV, SC, TX, VA, and WV. There was government distribution and no military distribution. Foreign distribution was made to Poland and Russia.
- Lot
- Lot numbers 1703221A and 1705111A
- Risk classification
- Class III
- Area (FDA)
- device
- Country
- United States
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